Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acap1 |
A |
G |
11: 69,773,517 (GRCm39) |
S431P |
possibly damaging |
Het |
Arid1b |
C |
A |
17: 5,387,385 (GRCm39) |
R1613S |
possibly damaging |
Het |
Atxn2l |
T |
C |
7: 126,097,460 (GRCm39) |
D196G |
possibly damaging |
Het |
Bag3 |
C |
A |
7: 128,148,065 (GRCm39) |
T560K |
probably benign |
Het |
BC051076 |
A |
G |
5: 88,112,354 (GRCm39) |
|
probably benign |
Het |
Becn1 |
A |
T |
11: 101,186,448 (GRCm39) |
M18K |
probably benign |
Het |
C130050O18Rik |
G |
A |
5: 139,400,493 (GRCm39) |
C182Y |
probably damaging |
Het |
Cfap43 |
A |
G |
19: 47,811,627 (GRCm39) |
|
probably benign |
Het |
Cfap97 |
C |
T |
8: 46,623,222 (GRCm39) |
S204L |
probably damaging |
Het |
Gaa |
A |
G |
11: 119,165,786 (GRCm39) |
T100A |
probably benign |
Het |
Gab2 |
C |
T |
7: 96,948,465 (GRCm39) |
P352S |
probably damaging |
Het |
Gckr |
T |
A |
5: 31,465,111 (GRCm39) |
I360N |
possibly damaging |
Het |
Gm4553 |
T |
C |
7: 141,718,964 (GRCm39) |
S155G |
unknown |
Het |
Gulo |
G |
T |
14: 66,243,398 (GRCm39) |
A40D |
probably damaging |
Het |
Irs1 |
T |
C |
1: 82,266,204 (GRCm39) |
I671V |
probably benign |
Het |
Itgax |
T |
C |
7: 127,747,481 (GRCm39) |
V1028A |
possibly damaging |
Het |
Lamb3 |
T |
C |
1: 193,002,755 (GRCm39) |
C67R |
probably damaging |
Het |
Nat8 |
C |
T |
6: 85,807,579 (GRCm39) |
V185M |
probably benign |
Het |
Ninj2 |
A |
C |
6: 120,175,023 (GRCm39) |
T65P |
probably benign |
Het |
Nrg2 |
T |
C |
18: 36,154,271 (GRCm39) |
M549V |
probably benign |
Het |
Nwd2 |
A |
G |
5: 63,962,818 (GRCm39) |
M801V |
probably benign |
Het |
Pde8b |
T |
C |
13: 95,170,875 (GRCm39) |
D589G |
probably damaging |
Het |
Ppp1r35 |
T |
A |
5: 137,777,799 (GRCm39) |
V155E |
probably damaging |
Het |
Prss36 |
T |
A |
7: 127,544,099 (GRCm39) |
|
probably benign |
Het |
Raver2 |
A |
G |
4: 100,960,065 (GRCm39) |
K182E |
probably damaging |
Het |
Ring1 |
T |
G |
17: 34,241,983 (GRCm39) |
E142A |
possibly damaging |
Het |
Sidt2 |
T |
A |
9: 45,853,534 (GRCm39) |
M689L |
possibly damaging |
Het |
Slc45a4 |
A |
G |
15: 73,459,504 (GRCm39) |
V95A |
probably damaging |
Het |
Ssc5d |
T |
C |
7: 4,947,480 (GRCm39) |
V1278A |
possibly damaging |
Het |
Stk36 |
A |
T |
1: 74,673,861 (GRCm39) |
K1251N |
possibly damaging |
Het |
Utp14b |
T |
A |
1: 78,642,262 (GRCm39) |
S53R |
probably damaging |
Het |
Vmn2r17 |
A |
T |
5: 109,575,858 (GRCm39) |
E243V |
probably benign |
Het |
|
Other mutations in Mpdz |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Mpdz
|
APN |
4 |
81,228,461 (GRCm39) |
nonsense |
probably null |
|
IGL00497:Mpdz
|
APN |
4 |
81,253,979 (GRCm39) |
missense |
probably benign |
0.30 |
IGL00502:Mpdz
|
APN |
4 |
81,287,960 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00539:Mpdz
|
APN |
4 |
81,279,588 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL00938:Mpdz
|
APN |
4 |
81,210,749 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00990:Mpdz
|
APN |
4 |
81,221,821 (GRCm39) |
splice site |
probably benign |
|
IGL01394:Mpdz
|
APN |
4 |
81,210,728 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01537:Mpdz
|
APN |
4 |
81,287,895 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01558:Mpdz
|
APN |
4 |
81,213,767 (GRCm39) |
nonsense |
probably null |
|
IGL01561:Mpdz
|
APN |
4 |
81,202,851 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01649:Mpdz
|
APN |
4 |
81,221,870 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01743:Mpdz
|
APN |
4 |
81,235,919 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01941:Mpdz
|
APN |
4 |
81,204,624 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01969:Mpdz
|
APN |
4 |
81,276,961 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02023:Mpdz
|
APN |
4 |
81,247,766 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02081:Mpdz
|
APN |
4 |
81,254,106 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02304:Mpdz
|
APN |
4 |
81,215,796 (GRCm39) |
splice site |
probably benign |
|
IGL02304:Mpdz
|
APN |
4 |
81,228,394 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02410:Mpdz
|
APN |
4 |
81,215,730 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02449:Mpdz
|
APN |
4 |
81,247,659 (GRCm39) |
splice site |
probably null |
|
IGL02671:Mpdz
|
APN |
4 |
81,208,510 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02708:Mpdz
|
APN |
4 |
81,202,808 (GRCm39) |
splice site |
probably null |
|
IGL02718:Mpdz
|
APN |
4 |
81,303,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03065:Mpdz
|
APN |
4 |
81,210,802 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03378:Mpdz
|
APN |
4 |
81,337,285 (GRCm39) |
splice site |
probably benign |
|
PIT4458001:Mpdz
|
UTSW |
4 |
81,337,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R0108:Mpdz
|
UTSW |
4 |
81,300,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R0108:Mpdz
|
UTSW |
4 |
81,300,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R0119:Mpdz
|
UTSW |
4 |
81,210,768 (GRCm39) |
missense |
probably benign |
0.44 |
R0402:Mpdz
|
UTSW |
4 |
81,279,677 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0499:Mpdz
|
UTSW |
4 |
81,210,768 (GRCm39) |
missense |
probably benign |
0.44 |
R0718:Mpdz
|
UTSW |
4 |
81,210,710 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0844:Mpdz
|
UTSW |
4 |
81,339,431 (GRCm39) |
start gained |
probably benign |
|
R0883:Mpdz
|
UTSW |
4 |
81,278,228 (GRCm39) |
splice site |
probably benign |
|
R0885:Mpdz
|
UTSW |
4 |
81,287,829 (GRCm39) |
missense |
probably benign |
0.04 |
R1344:Mpdz
|
UTSW |
4 |
81,226,556 (GRCm39) |
missense |
probably benign |
0.01 |
R1432:Mpdz
|
UTSW |
4 |
81,210,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R1488:Mpdz
|
UTSW |
4 |
81,266,945 (GRCm39) |
nonsense |
probably null |
|
R1589:Mpdz
|
UTSW |
4 |
81,339,413 (GRCm39) |
missense |
probably benign |
0.00 |
R1756:Mpdz
|
UTSW |
4 |
81,225,114 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1940:Mpdz
|
UTSW |
4 |
81,279,680 (GRCm39) |
missense |
probably benign |
0.01 |
R2068:Mpdz
|
UTSW |
4 |
81,254,067 (GRCm39) |
missense |
probably null |
1.00 |
R2182:Mpdz
|
UTSW |
4 |
81,266,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R2213:Mpdz
|
UTSW |
4 |
81,228,409 (GRCm39) |
missense |
probably damaging |
0.99 |
R2265:Mpdz
|
UTSW |
4 |
81,301,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R2268:Mpdz
|
UTSW |
4 |
81,301,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R2269:Mpdz
|
UTSW |
4 |
81,301,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R3082:Mpdz
|
UTSW |
4 |
81,203,695 (GRCm39) |
splice site |
probably benign |
|
R3746:Mpdz
|
UTSW |
4 |
81,281,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R3902:Mpdz
|
UTSW |
4 |
81,225,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R4095:Mpdz
|
UTSW |
4 |
81,302,060 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4097:Mpdz
|
UTSW |
4 |
81,253,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R4206:Mpdz
|
UTSW |
4 |
81,299,999 (GRCm39) |
missense |
probably benign |
0.13 |
R4675:Mpdz
|
UTSW |
4 |
81,302,049 (GRCm39) |
missense |
probably damaging |
0.98 |
R4884:Mpdz
|
UTSW |
4 |
81,279,713 (GRCm39) |
missense |
probably damaging |
0.97 |
R5044:Mpdz
|
UTSW |
4 |
81,299,934 (GRCm39) |
missense |
probably benign |
0.16 |
R5050:Mpdz
|
UTSW |
4 |
81,213,685 (GRCm39) |
missense |
probably benign |
0.00 |
R5243:Mpdz
|
UTSW |
4 |
81,225,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R5332:Mpdz
|
UTSW |
4 |
81,210,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R5435:Mpdz
|
UTSW |
4 |
81,201,724 (GRCm39) |
intron |
probably benign |
|
R5720:Mpdz
|
UTSW |
4 |
81,205,931 (GRCm39) |
missense |
probably damaging |
0.99 |
R5743:Mpdz
|
UTSW |
4 |
81,339,425 (GRCm39) |
start codon destroyed |
probably null |
0.30 |
R5764:Mpdz
|
UTSW |
4 |
81,274,683 (GRCm39) |
missense |
probably benign |
0.13 |
R5876:Mpdz
|
UTSW |
4 |
81,203,711 (GRCm39) |
nonsense |
probably null |
|
R5938:Mpdz
|
UTSW |
4 |
81,202,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R5988:Mpdz
|
UTSW |
4 |
81,202,812 (GRCm39) |
critical splice donor site |
probably null |
|
R6125:Mpdz
|
UTSW |
4 |
81,215,764 (GRCm39) |
missense |
probably benign |
0.00 |
R6178:Mpdz
|
UTSW |
4 |
81,226,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R6235:Mpdz
|
UTSW |
4 |
81,303,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R6293:Mpdz
|
UTSW |
4 |
81,278,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R6387:Mpdz
|
UTSW |
4 |
81,299,946 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6488:Mpdz
|
UTSW |
4 |
81,205,970 (GRCm39) |
missense |
probably benign |
0.11 |
R6536:Mpdz
|
UTSW |
4 |
81,301,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R6673:Mpdz
|
UTSW |
4 |
81,274,667 (GRCm39) |
missense |
probably benign |
0.11 |
R6879:Mpdz
|
UTSW |
4 |
81,266,893 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7180:Mpdz
|
UTSW |
4 |
81,253,988 (GRCm39) |
missense |
probably damaging |
0.98 |
R7199:Mpdz
|
UTSW |
4 |
81,215,570 (GRCm39) |
missense |
probably damaging |
0.98 |
R7209:Mpdz
|
UTSW |
4 |
81,225,114 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7309:Mpdz
|
UTSW |
4 |
81,300,195 (GRCm39) |
splice site |
probably null |
|
R7359:Mpdz
|
UTSW |
4 |
81,274,632 (GRCm39) |
missense |
probably benign |
0.01 |
R7561:Mpdz
|
UTSW |
4 |
81,225,388 (GRCm39) |
missense |
probably damaging |
0.99 |
R7565:Mpdz
|
UTSW |
4 |
81,221,891 (GRCm39) |
missense |
probably benign |
0.01 |
R7738:Mpdz
|
UTSW |
4 |
81,253,986 (GRCm39) |
missense |
probably benign |
0.01 |
R7941:Mpdz
|
UTSW |
4 |
81,200,987 (GRCm39) |
missense |
probably benign |
0.04 |
R8074:Mpdz
|
UTSW |
4 |
81,267,324 (GRCm39) |
missense |
probably benign |
0.00 |
R8957:Mpdz
|
UTSW |
4 |
81,251,216 (GRCm39) |
nonsense |
probably null |
|
R8998:Mpdz
|
UTSW |
4 |
81,202,882 (GRCm39) |
nonsense |
probably null |
|
R8999:Mpdz
|
UTSW |
4 |
81,202,882 (GRCm39) |
nonsense |
probably null |
|
R9001:Mpdz
|
UTSW |
4 |
81,299,999 (GRCm39) |
missense |
probably benign |
|
R9223:Mpdz
|
UTSW |
4 |
81,202,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R9415:Mpdz
|
UTSW |
4 |
81,235,905 (GRCm39) |
nonsense |
probably null |
|
R9486:Mpdz
|
UTSW |
4 |
81,254,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R9520:Mpdz
|
UTSW |
4 |
81,304,555 (GRCm39) |
missense |
probably benign |
|
R9526:Mpdz
|
UTSW |
4 |
81,274,653 (GRCm39) |
missense |
probably benign |
|
R9556:Mpdz
|
UTSW |
4 |
81,278,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R9722:Mpdz
|
UTSW |
4 |
81,304,504 (GRCm39) |
missense |
probably damaging |
0.97 |
RF013:Mpdz
|
UTSW |
4 |
81,211,829 (GRCm39) |
missense |
possibly damaging |
0.60 |
X0011:Mpdz
|
UTSW |
4 |
81,210,996 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Mpdz
|
UTSW |
4 |
81,238,727 (GRCm39) |
missense |
probably damaging |
0.99 |
|